| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 164501 | BAA02g10950 | A02 | 4923993 | G | A | upstream_gene_variant | MODIFIER | c.-1799G>A| |
S17 |
| 164502 | BAA02g10950 | A02 | 4924723 | C | T | upstream_gene_variant | MODIFIER | c.-1069C>T| |
S242 |
| 164503 | BAA02g10950 | A02 | 4925865 | C | T | missense_variant | MODERATE | c.74C>T|p.Ser25Phe |
S38 |
| 164504 | BAA02g10960 | A02 | 4926392 | C | T | missense_variant | MODERATE | c.244G>A|p.Val82Met |
S293 |
| 164505 | BAA02g10960 | A02 | 4928158 | G | A | upstream_gene_variant | MODIFIER | c.-1523C>T| |
S282 |
| 164506 | BAA02g10960 | A02 | 4928988 | C | T | upstream_gene_variant | MODIFIER | c.-2353G>A| |
S250 |
| 164507 | BAA02g10960 | A02 | 4931240 | G | A | upstream_gene_variant | MODIFIER | c.-4605C>T| |
S239 |
| 164508 | BAA02g10960 | A02 | 4931521 | G | A | upstream_gene_variant | MODIFIER | c.-4886C>T| |
S67 |
| 164509 | BAA02g10970 | A02 | 4932415 | C | T | upstream_gene_variant | MODIFIER | c.-2646C>T| |
S172 S217 |
| 164510 | BAA02g10970 | A02 | 4932734 | C | T | upstream_gene_variant | MODIFIER | c.-2327C>T| |
S305 |
| 164511 | BAA02g10970 | A02 | 4932821 | C | T | upstream_gene_variant | MODIFIER | c.-2240C>T| |
S100 |
| 164512 | BAA02g10970 | A02 | 4932934 | G | A | upstream_gene_variant | MODIFIER | c.-2127G>A| |
S153 S213 |
| 164513 | BAA02g10970 | A02 | 4933825 | G | A | upstream_gene_variant | MODIFIER | c.-1236G>A| |
S303 |
| 164514 | BAA02g10970 | A02 | 4934339 | G | A | upstream_gene_variant | MODIFIER | c.-722G>A| |
S207 |
| 164515 | BAA02g10970 | A02 | 4934400 | G | A | upstream_gene_variant | MODIFIER | c.-661G>A| |
S56 |
| 164516 | BAA02g10970 | A02 | 4935236 | C | T | missense_variant | MODERATE | c.176C>T|p.Pro59Leu |
S267 |
| 164517 | BAA02g10970 | A02 | 4935472 | G | A | missense_variant | MODERATE | c.412G>A|p.Glu138Lys |
S92 |
| 164518 | BAA02g10970 | A02 | 4935604 | G | A | missense_variant | MODERATE | c.454G>A|p.Asp152Asn |
S282 |
| 164519 | BAA02g10970 | A02 | 4936323 | G | A | missense_variant | MODERATE | c.682G>A|p.Glu228Lys |
S283 |
| 164520 | BAA02g10980 | A02 | 4938376 | G | A | upstream_gene_variant | MODIFIER | c.-2346G>A| |
S91 |
| 164521 | BAA02g10980 | A02 | 4939744 | G | A | upstream_gene_variant | MODIFIER | c.-978G>A| |
S107 |
| 164522 | BAA02g10980 | A02 | 4940101 | C | T | upstream_gene_variant | MODIFIER | c.-621C>T| |
S251 |
| 164523 | BAA02g10980 | A02 | 4940302 | G | A | upstream_gene_variant | MODIFIER | c.-420G>A| |
S159 S243 |
| 164524 | BAA02g10980 | A02 | 4940323 | C | T | upstream_gene_variant | MODIFIER | c.-399C>T| |
S34 |
| 164525 | BAA02g10980 | A02 | 4940570 | G | A | upstream_gene_variant | MODIFIER | c.-152G>A| |
S247 |